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NRC Publications Archive Archives des publications du CNRCThis publication could be one of several versions: author's original, accepted manuscript or the publisher's version. / La version de cette publication peut être l'une des suivantes : la version prépublication de l'auteur, la version acceptée du manuscrit ou la version de l'éditeur. For the publisher's version, please access the DOI link below./ Pour consulter la version de l'éditeur, utilisez le lien DOI ci-dessous.http://dx.doi.org/10.1016/j.memsci.2013.06.003 Science, 445, pp. 220-227, 2013-06-13 Polyamide thin-film composite membranes based on carboxylated polysulfone microporous support membranes for forward osmosis Cho, Young Hoon; Han, Jungim; Han, Sungsoo; Guiver, Michael D.; Park, Ho Bum
Journal of Membrane
AbstractDue to its simple process and low energy consumption, forward osmosis (FO) has gained significant attention in the fields of emergency drinks, desalination, landfill leachate treatment, and brine concentration. However, current state-of-the-art reverse osmosis (RO) membranes show relatively low water fluxes in FO processes due to high internal concentration polarization (ICP) and high mass transfer resistance in commercially available microporous support membranes. In this study, carboxylated polysulfones (CPSFs) were synthesized via direct polysulfone (PSF) functionalization and considered as moderately hydrophilic, mechanically stable microporous support membranes. The incorporation of hydrophilic groups into hydrophobic polymer backbones often reduces mechanical strength due to excessive water swelling. However, the mechanical properties of CPSFs (degree of substitution, DS=0.45~0.85) were similar to those of pristine PSF, and they retained their hydrophilic nature. Microporous CPSF membranes were prepared in various conditions, and FO water fluxes and salt passages of polyamide thin-film/CPSF composite membranes were measured and compared with each other. CPSF-based FO membranes showed significantly higher water fluxes than PSF-based FO membranes at the same membrane formation conditions, which might be due to enhanced hydrophilicity and reduced ICP.